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	1.	R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease? [electronic resource] by López-Bigas, N Rabionet, R Arbonés, M L Estivill, X Producer: 20010405 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Gene targeting in normal somatic cells: inactivation of the interferon-gamma receptor in myoblasts. [electronic resource] by Arbonés, M L Austin, H A Capon, D J Greenburg, G Producer: 19940425 In: Nature genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Murine models for Down syndrome. [electronic resource] by Dierssen, M Fillat, C Crnic, L Arbonés, M Flórez, J Estivill, X Producer: 20011204 In: Physiology & behavior vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Haploinsufficiency of Dyrk1A in mice leads to specific alterations in the development and regulation of motor activity. [electronic resource] by Fotaki, V Martínez De Lagrán, M Estivill, X Arbonés, M Dierssen, M Producer: 20040920 In: Behavioral neuroscience vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Neurobehavioral development of two mouse lines commonly used in transgenic studies. [electronic resource] by Dierssen, M Fotaki, V Martínez de Lagrán, M Gratacós, M Arbonés, M Fillat, C Estivill, X Producer: 20021231 In: Pharmacology, biochemistry, and behavior vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Characteristics of nitric oxide synthase type I of rat cerebellar astrocytes. [electronic resource] by Arbonés, M L Ribera, J Agulló, L Baltrons, M A Casanovas, A Riveros-Moreno, V García, A Producer: 19970304 In: Glia vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson's disease. [electronic resource] by Barallobre, M J Perier, C Bové, J Laguna, A Delabar, J M Vila, M Arbonés, M L Producer: 20150212 In: Cell death & disease vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) gene. [electronic resource] by López-Bigas, N Rabionet, R Martínez, E Banchs, I Volpini, V Vance, J M Arbonés, M L Estivill, X Producer: 20000921 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome. [electronic resource] by López-Bigas, N Rabionet, R de Cid, R Govea, N Gasparini, P Zelante, L Arbonés, M L Estivill, X Producer: 20000124 In: Human mutation vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Sequential contribution of L- and P-selectin to leukocyte rolling in vivo. [electronic resource] by Ley, K Bullard, D C Arbonés, M L Bosse, R Vestweber, D Tedder, T F Beaudet, A L Producer: 19950224 In: The Journal of experimental medicine vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Coxsackie adenovirus receptor and alpha nu beta3/alpha nu beta5 integrins in adenovirus gene transfer of rat cochlea. [electronic resource] by Venail, F Wang, J Ruel, J Ballana, E Rebillard, G Eybalin, M Arbones, M Bosch, A Puel, J-L Producer: 20070716 In: Gene therapy vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutations in the mitochondrial tRNA Ser(UCN) and in the GJB2 (connexin 26) gene are not modifiers of the age at onset or severity of hearing loss in Spanish patients with the 12S rRNA A1555G mutation. [electronic resource] by López-Bigas, N Rabionet, R Martinez, E Bravo, O Girons, J Borragan, A Pellicer, M Arbonés, M L Estivill, X Producer: 20000531 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. [electronic resource] by Rabionet, R Zelante, L López-Bigas, N D'Agruma, L Melchionda, S Restagno, G Arbonés, M L Gasparini, P Estivill, X Producer: 20000922 In: Human genetics vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice. [electronic resource] by Arbonés, M L Ord, D C Ley, K Ratech, H Maynard-Curry, C Otten, G Capon, D J Tedder, T F Producer: 19950418 In: Immunity vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Functional genomics of Down syndrome: a multidisciplinary approach. [electronic resource] by Dierssen, M Martí, E Pucharcós, C Fotaki, V Altafaj, X Casas, K Solans, A Arbonés, M L Fillat, C Estivill, X Producer: 20020610 In: Journal of neural transmission. Supplementum no. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment. [electronic resource] by López-Bigas, N Melchionda, S de Cid, R Grifa, A Zelante, L Govea, N Arbonés, M L Gasparini, P Estivill, X Producer: 20020805 In: Human mutation vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Dopaminergic deficiency in mice with reduced levels of the dual-specificity tyrosine-phosphorylated and regulated kinase 1A, Dyrk1A(+/-). [electronic resource] by Martinez de Lagran, M Bortolozzi, A Millan, O Gispert, J D Gonzalez, J R Arbones, M L Artigas, F Dierssen, M Producer: 20071106 In: Genes, brain, and behavior vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment. [electronic resource] by López-Bigas, N Melchionda, S de Cid, R Grifa, A Zelante, L Govea, N Arbonés, M L Gasparini, P Estivill, X Producer: 20020307 In: Human mutation vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome. [electronic resource] by Pucharcós, C Fuentes, J J Casas, C de la Luna, S Alcántara, S Arbonés, M L Soriano, E Estivill, X Pritchard, M Producer: 19991101 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/- mouse. [electronic resource] by Benavides-Piccione, R Dierssen, M Ballesteros-Yáñez, I Martínez de Lagrán, M Arbonés, M L Fotaki, V DeFelipe, J Elston, G N Producer: 20051219 In: Neurobiology of disease vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 26 results.